Canonical Allele Identifier: CA1405402195
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945851_138945868delinsTGGGGGTGCGGCGGAGGC , CM000665.2:g.138945851_138945868delinsTGGGGGTGCGGCGGAGGC GRCh38
NC_000003.11:g.138664693_138664710delinsTGGGGGTGCGGCGGAGGC , CM000665.1:g.138664693_138664710delinsTGGGGGTGCGGCGGAGGC GRCh37
NC_000003.10:g.140147383_140147400delinsTGGGGGTGCGGCGGAGGC NCBI36
NG_012454.1:g.6273_6290delinsGCCTCCGCCGCACCCCCA
NG_029796.1:g.3618_3635delinsTGGGGGTGCGGCGGAGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.855_872delinsGCCTCCGCCGCACCCCCA MANE Select ENSP00000497217.1:p.Pro285=
ENST00000330315.3:c.855_872delinsGCCTCCGCCGCACCCCCA ENSP00000333188.3:p.Pro285=
NM_023067.3:c.855_872delinsGCCTCCGCCGCACCCCCA NP_075555.1:p.Pro285=
NM_023067.4:c.855_872delinsGCCTCCGCCGCACCCCCA MANE Select NP_075555.1:p.Pro285=
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